Canonical Allele Identifier: CA2014025871
Gene: TNFRSF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6333098T= , CM000674.2:g.6333098T= GRCh38
NC_000012.11:g.6442264T= , CM000674.1:g.6442264T= GRCh37
NC_000012.10:g.6312525T= NCBI36
NG_007506.1:g.13998A= , LRG_193:g.13998A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366159.9:n.556A=
ENST00000437813.8:c.522A= ENSP00000513672.1:p.Leu174=
ENST00000440083.7:c.741A= ENSP00000413224.3:p.Leu247=
ENST00000535958.2:c.*349A= ENSP00000513673.1:n.*349A=
ENST00000698339.1:c.522A= ENSP00000513670.1:p.Leu174=
ENST00000698340.1:c.522A= ENSP00000513671.1:p.Leu174=
ENST00000162749.7:c.522A= MANE Select ENSP00000162749.2:p.Leu174=
ENST00000162749.6:c.522A= ENSP00000162749.2:p.Leu174=
ENST00000366159.8:c.522A= ENSP00000380389.3:p.Leu174=
ENST00000437813.7:n.483A=
ENST00000440083.6:c.741A= ENSP00000413224.2:p.Leu247=
ENST00000534885.5:c.368A= ENSP00000441803.1:p.Ter123=
ENST00000537842.5:n.126A=
ENST00000539372.5:c.522A= ENSP00000442059.1:p.Leu174=
ENST00000540022.5:c.393A= ENSP00000438343.1:p.Leu131=
ENST00000543048.5:c.*133A= ENSP00000439981.1:n.*133A=
ENST00000543359.5:n.8A=
ENST00000543995.5:c.*109A= ENSP00000442405.1:n.*109A=
NM_001065.3:c.522A= , LRG_193t1:c.522A= NP_001056.1:p.Leu174=
NM_001346091.1:c.198A= NP_001333020.1:p.Leu66=
NM_001346092.1:c.-56A= NP_001333021.1:n.-56A=
NR_144351.1:n.825A=
NM_001065.4:c.522A= MANE Select NP_001056.1:p.Leu174=
NM_001346091.2:c.198A= NP_001333020.1:p.Leu66=
NM_001346092.2:c.-56A= NP_001333021.1:n.-56A=
NR_144351.2:n.784A=